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nsv6897864

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,119

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 232 SVs from 47 studies. See in: genome view    
    Submitted genomic30,839,815-30,933,933Question Mark
    Overlapping variant regions from other studies: 232 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):31,128,744-31,222,862Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897864Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1030,839,81530,933,933
    nsv6897864RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1031,128,74431,222,862

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18580516duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18580516Submitted genomicNC_000010.11:g.308
    39815_30933933dup
    GRCh38 (hg38)NC_000010.11Chr1030,839,81530,933,933
    nssv18580516RemappedPerfectNC_000010.10:g.311
    28744_31222862dup
    GRCh37.p13First PassNC_000010.10Chr1031,128,74431,222,862

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv185805162.8e-058275756
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